3bg8

Disease
Known disease associated with this structure: Factor XI deficiency, autosomal dominant OMIM:[264900], Factor XI deficiency, autosomal recessive OMIM:[264900]

About this Structure
3BG8 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference
Clavatadine A, a natural product with selective recognition and irreversible inhibition of factor XIa., Buchanan MS, Carroll AR, Wessling D, Jobling M, Avery VM, Davis RA, Feng Y, Xue Y, Oster L, Fex T, Deinum J, Hooper JN, Quinn RJ, J Med Chem. 2008 Jun 26;51(12):3583-7. PMID:18510371

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